Znn3bq.jpeg
²é¿´: 327  |  »Ø¸´: 2

haijiaotang

Òø³æ (ÕýʽдÊÖ)

[ÇóÖú] ΢Æ×ÇóÖúÒ»ÏÂÊý¾ÝµÄ»¯ºÏÎï

̼Æ×Êý¾ÝÈçÏ £ºÈܼÁ MEOD
18.0,21.0,21.5,21.5,23.8,27.4,28.9,29.7,31.8,32.5,33.6,35.9,39.6,42.4,43.0,50.5,57.5,71.3,72.1,75.4,77.9,78.4,85.8,121.8,167.8,204.3
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

ÌìÏÂÎÞË«ts

ľ³æ (ÕýʽдÊÖ)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
²éѯ½á¹û£º¹²²éµ½3718¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     2-deoxy-3-epi-4¦Â,20-dihydroxyecdysone
    ÏàËÆ¶È:92.3%
Russian Chemical Bulletin          2000          49          1923-1924
A new phytoecdysteroid
V. N. Odinokov, I. V. Galyautdinov, A. A. Fatykhov and L. M. Khalilov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     1¦Á,20R-hydroxyecdysone
    ÏàËÆ¶È:81.4%
Natural Product Research and Development          2002          14(1)          9-12
STUDY ON THE CHEMICAL CONSTITUENTS OF LYCHNIS CORONARIA
DAI Hao-fu; LIU Yu-qing; DENG Shi-ming; TAN Ning-hua; ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     20-hydroxyecdysone
    ÏàËÆ¶È:81.4%
Food Chemistry          2005          92          125-132
Nutritional and antinutritional composition of Kancolla seeds: an interesting and underexploited andine food plant
Irene Dini, Gian Carlo Tenore, Antonio Dini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     2-È¥Ñõ¼×¿ÇçÞͪ
    ÏàËÆ¶È:81.4%
Journal of Chinese Medicinal Materials          2010          33          1574-1576
Studies on the Chemical Constituents from the Roots of Tinospora sagittata var. yunnanensis(¢ò)
HUANG Xiang-zhong, CHENG Chun-mei, YIN Yan, GUO Jun-ming, LIANG Hui, DAI Yun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     20-hydroxyecdysone
    ÏàËÆ¶È:80.7%
Steroids          2002          67          127-135
Photochemical transformation of 20-hydroxyecdysone: production of monomeric and dimeric ecdysteroid analogues
Juraj Harmatha, Miloš Budĕš¨ªnsky, Karel Vok¨¢ĕ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     20-hydroxyecdysone
C27H44O7     ÏàËÆ¶È:80.7%
Phytochemistry          1998          49          2109-2114
Ecdysteroid constituents of the mushroom Tapinella panuoides
Karel Vok¨¢, Milo Budnsky, Juraj Harmath¦Á, Jitka Kohoutov¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     20-hydroxy-ecdysone
    ÏàËÆ¶È:80.7%
Phytochemistry          1994          37          707-711
Ecdysteroids from the roots of Leuzea carthamoides
Jaroslav P¨ªš, Miloš Bud¨§š¨ªnsky̌, Karel Vok¨¢č, V¨§ra Laudov¨¢, Juraj Harmatha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     20-hydroxyecdysone
    ÏàËÆ¶È:80.7%
Tetrahedron          1998          54          1657-1666
New ergostane type ecdysteroids from fungi. Ecdysteroid constituents of mushroom Paxillus atrotomentosus
Karel Vok¨¢č, Miloš Bud¨§š¨ªnsky, Juraj Harmatha, Jaroslav P¨ªš
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     2'-hydroxyecdysone
    ÏàËÆ¶È:77.7%
Phytochemistry          2003                   1179-1184
Ecdysteroids and other constituents from Sida spinosa L.
Faten M.M. Darwish, Manfred G. Reinecke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     integristerone A
    ÏàËÆ¶È:77.7%
Helvetica Chimica Acta          2009          92          753-761
Ecdysteroids from Silene viridiflora
Andr¨¢s Simon, No¨¦mi T¨®th, G¨¢bor T¨®th, Zolt¨¢n Kele, Judit Groska, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     integristerone A
    ÏàËÆ¶È:77.7%
Steroids          2004          69          389-394
A new ecdysteroid with unique 9¦Â-OH and four other ecdysteroids from Silene italica ssp. nemoralis
Andr¨¢s Simon, Zita Pongr¨¢cz, G¨¢bor T¨®th, Marianna M¨¢k, Imre M¨¢th¨¦, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     20-Hydroxyecdysone
    ÏàËÆ¶È:77.7%
Steroids          2008          73          502-514
Additional minor ecdysteroid components of Leuzea carthamoides
Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     20-hydroxyecdysone
    ÏàËÆ¶È:77.7%
China Journal of Chinese Materia Medica          2003          28          730-732
Studies on Chemical Constituents in Herb of Lamium maculatum L. var Kansuense
DENG Yanru, HE Li, LI Weiqi, WANG Hanqing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     20-hydroxyecdysone
    ÏàËÆ¶È:77.7%
Phytochemistry          1997          44          513-521
Ecdysteroid xylosides from Limnanthes douglasii
Satyajit D. Sarker, Jean-Pierre Girault, Ren¨¦ Lafont, Laurence N. Dinan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     ¦Â-ecdysone
C27H44O7     ÏàËÆ¶È:77.7%
Journal of Natural Medicines          2010          64          114-116
New naphthoquinone from the root of Lygodium japonicum (Thunb.) Sw.
Lijuan Chen, Guogang Zhang, Jie He, Jin Guan and Chunyuan Pan, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     ¦Â-ecdysone
C27H44O7     ÏàËÆ¶È:77.7%
Chinese Traditional and Herbal Drugs          2006          37          1304-1306
°Î¶¾É¢»¯Ñ§³É·ÖµÄÑо¿
Àîά·å;ËÎÆôʾ;Ïîΰ;ÑîÊçÃô
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     ¦Â-ecdysterone
C27H44O7     ÏàËÆ¶È:77.7%
Journal of China Pharmaceutical University          2006          37          487-490
Chemical constituents from Asparagus filicinus
WU Jia-jun; WANG Hao; YE Wen-cai; ZUO Xiao-feng; ZHAO Shou-xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     ¦Â-ecdysterone
C27H44O7     ÏàËÆ¶È:77.7%
Asian Journal of Traditional Medicines          2006          1          7-10
Anti-tumor Constituents from Paris polyphylla
Yu Wang , Wenyuan Gao , Xinqiao Liu , Yutong Zuo , Haixia Chen, and Hongquan Duan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     2¦Â,3¦Â,14¦Á,20¦Â,22¦Á,25-hexahydroxy-5¦Â-cholest-7-en-6-one
C27H44O7     ÏàËÆ¶È:77.7%
Indian Journal of Chemistry          1995          34B          674-676
NMR studies of 20¦Â-hydroxyecdysone,a steroid;isolated from Tinospora cordifolia
A shish K Pathak, Pawan K Agariwal, Dharam C Jain, Ram P Sharma & Oliver W Howarth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     Ecdysterone
    ÏàËÆ¶È:76.9%
Journal of Natural Products          1995          Vol 58          264-268
4-Dehydroecdysterone, a New Ecdysteroid from the Zoanthid Parazoanthus sp.
Philip A. Searle, Tadeusz F. Molinski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     20-Hydroxyecdysone 2-acetate
C29H46O8     ÏàËÆ¶È:75.8%
Steroids          2008          73          502-514
Additional minor ecdysteroid components of Leuzea carthamoides
Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     2-deoxy-20-hydroxyecdysone
    ÏàËÆ¶È:74.0%
Helvetica Chimica Acta          2009          92          753-761
Ecdysteroids from Silene viridiflora
Andr¨¢s Simon, No¨¦mi T¨®th, G¨¢bor T¨®th, Zolt¨¢n Kele, Judit Groska, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     20-hydroxyecdysone
    ÏàËÆ¶È:74.0%
Korean Journal of Pharmacognosy          1999          30(3)          335-339
Isolatin and Quantitative Determination of 20-Hydroxyecdysone from Achyranthis Radix
Hwang, Ji-Hyun; Lee, Seung-Ho; Park, Jeong-Hill; Kang, Shin-Jung; Chang, Seung-Yeup; Lee, Kyong-Soon; Son, Kun-Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     Ecdysterone
    ÏàËÆ¶È:74.0%
Chemistry of Natural Compounds          2010          46          173-175
A new alloside from Neocheiropteris palmatopedata
Ye-Gao Chen, Jian-Hong Yang, Yan Zhang and Ying Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     20¦Â-hydroxy-ecdysone
    ÏàËÆ¶È:74.0%
Natural Product Research and Development          2005          17          125-127
Chemical Constituents of Tinospora craveniana
LI Hong-bo; HU Jun; CHEN Jian-chao; QIU Ming-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     cholest-7-en-2¦Â,3¦Â,14¦Á,20¦Â,22¦Á,25-hexahydroxy-6-one
C27H44O7     ÏàËÆ¶È:74.0%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2003          42(5)          51-53
Polyhydroxylated Sterols from the Soft Coral Sinularia depressa
ZHANG Guang-wen, MA Xiang-quan, SU Jing-yu, ZENG Long-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     20-hydroxyecdysone
    ÏàËÆ¶È:73.0%
Phytochemistry          1997          46          103-105
24(241)[Z]-dehydroamarasterone B, a phytoecdysteroid from seeds of Leuzea carthamoides
U. A. Baltayev, L. Dinan, J. -P. Girault, R. Lafont
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     ¦Â-ecdysterone
    ÏàËÆ¶È:73.0%
Natural Product Research and Development          2003          15          93-97
ECDYSTEROIDS FROM THE STEMS OF DIPLOCLISIA GLAUCESCENS
HUANG Xiao chun GUO Yue wei ZHOU Wen liang ZUO Jian ping WANG Zheng tao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     3-Deoxy-1¦Â ,20-dihydroxyecdysone
C27H44O7     ÏàËÆ¶È:70.3%
Steroids          2002          67          555-558
3-Deoxy-1¦Â,20-dihydroxyecdysone from the leaves of Diploclisia glaucescens
Lalith Jayasinghe, Champika P. Jayasooriya, Kiyoshi Oyama, Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     polypodine B
    ÏàËÆ¶È:70.3%
China Journal of Chinese Materia Medica          2005          30          272-274
Studies on chemical constituents in herb of Lamium maculatum var. kansuense
DENG Yanru, DING Lan, WU Shuixian, WANG Hanqing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     polypodine B
    ÏàËÆ¶È:70.3%
Phytochemistry          1994          37          707-711
Ecdysteroids from the roots of Leuzea carthamoides
Jaroslav P¨ªš, Miloš Bud¨§š¨ªnsky̌, Karel Vok¨¢č, V¨§ra Laudov¨¢, Juraj Harmatha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     20¦Â-hydroxy-ecdysone-2-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:70.3%
Natural Product Research and Development          2005          17          125-127
Chemical Constituents of Tinospora craveniana
LI Hong-bo; HU Jun; CHEN Jian-chao; QIU Ming-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     polypodingB
    ÏàËÆ¶È:70.3%
Natural Product Research and Development          2002          14(1)          9-12
STUDY ON THE CHEMICAL CONSTITUENTS OF LYCHNIS CORONARIA
DAI Hao-fu; LIU Yu-qing; DENG Shi-ming; TAN Ning-hua; ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     Inokosterone 20,22-acetonide
C30H48O7     ÏàËÆ¶È:70%
Steroids          2008          73          502-514
Additional minor ecdysteroid components of Leuzea carthamoides
Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     2-deoxyintegristerone A
    ÏàËÆ¶È:69.2%
Helvetica Chimica Acta          2009          92          753-761
Ecdysteroids from Silene viridiflora
Andr¨¢s Simon, No¨¦mi T¨®th, G¨¢bor T¨®th, Zolt¨¢n Kele, Judit Groska, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     (20R,22R)-20,22-Dihydroxycholest-5-ene
C27H46O3     ÏàËÆ¶È:69.2%
Steroids          2008          73          1452-1464
Synthesis of ponasterone A derivatives with various steroid skeleton moieties and evaluation of their binding to the ecdysone receptor of Kc cells
Hirokazu Arai, Bunta Watanabe, Yoshiaki Nakagawa, Hisashi Miyagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     ponasterone A
C27H44O6     ÏàËÆ¶È:69.2%
Phytochemistry          1998          49          2109-2114
Ecdysteroid constituents of the mushroom Tapinella panuoides
Karel Vok¨¢, Milo Budnsky, Juraj Harmath¦Á, Jitka Kohoutov¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     turkesterone
C27H44O8     ÏàËÆ¶È:69.2%
Phytochemistry          1998          49          2109-2114
Ecdysteroid constituents of the mushroom Tapinella panuoides
Karel Vok¨¢, Milo Budnsky, Juraj Harmath¦Á, Jitka Kohoutov¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     ponasterone A
    ÏàËÆ¶È:69.2%
Russian Journal of Organic Chemistry          2002          38          525-529
Ozonolysis of Alkenes and Study of Reactions of Polyfunctional Compounds: LXVI.2* Ozonolysis and Hydrogenation of Diacetonides of 24,25- and 25,26-Anhydro-20-hydroxyecdysones. Synthesis of Ponasterone A
V. N. Odinokov, R. G. Savchenko, S. R. Nazmeeva, I. V. Galyautdinov and L. M. Khalilov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     11¦Â-hydroxy-20-deoxyshidasterone
C27H42O6     ÏàËÆ¶È:69.2%
Planta Medica          2013          79          52-59
Phytoecdysteroids from the Stem Bark of Vitex doniana and Their Anti-Inflammatory Effects
Ochieng, Charles O.; Ishola, Ismail O.; Opiyo, Sylvia A.; Manguro, Lawrence A.O.; Owuor, Philip O.; Wong, Keng-Chong:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     20-hydroxyecdysone 2,3-monoacetonide
    ÏàËÆ¶È:68.9%
Phytochemistry          1994          37          707-711
Ecdysteroids from the roots of Leuzea carthamoides
Jaroslav P¨ªš, Miloš Bud¨§š¨ªnsky̌, Karel Vok¨¢č, V¨§ra Laudov¨¢, Juraj Harmatha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     24-epimakisterone A
    ÏàËÆ¶È:67.8%
Chemistry & Biodiversity          2008          Vol. 5          707
Ecdysteroids from Vitex Species: Distribution and Compilation of Their 20C-NMR Spectral Data
Jos¨¦ G. Sena Filho, Jennifer Duringer, Gabriela L. A. Maia, Josean F. Tavares, Haroudo S. Xavier, Marcelo Sobral da Silva, Em.dio V. L. da-Cunha, and Jos¨¦ M. Barbosa-Filho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     24-epi-makisterone A
    ÏàËÆ¶È:67.8%
Planta Medica          1985          51          40-42
Phytoecdysteroids of Diploclisia glaucescens Seed
R. W. Miller, J. C1ardy, J. Kozlowski, K. L. Mikolajczak, R. D. Plattner, R. G. Powell, C. R. Smith, D. Weisleder and Zheng Qi-Tai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     24-epi-makisterone A
C28H46O7     ÏàËÆ¶È:67.8%
Chinese Traditional and Herbal Drugs          2001          32          12-13
Isolation and identification of non alkaloid components from Tinospora hainanensis (¢ó)
LIN Lian bo; FU Xiao wen; GUO You ying; Keisuke KOJIMA; Ykio OGIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     24-Epi-makisterone A
    ÏàËÆ¶È:67.8%
Journal of Agricultural and Food Chemistry          2001          49          2576-2578
Ecdysteroids of Quinoa Seeds (Chenopodium quinoa Willd.)
Nanqun Zhu, Hiroe Kikuzaki, Bret C. Vastano, Nobuji Nakatani, Mukund V. Karwe, Robert T. Rosen, and Chi-Tang Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     Polypodine B 2-¦Â-D-glucoside
C33H54O13     ÏàËÆ¶È:67.7%
Steroids          2011          76          1419-1424
Ecdysteroids from Polypodium vulgare L.
Andr¨¢s Simon, Attila V¨¢nyol¨®s, Zolt¨¢n B¨¦ni, Mikl¨®s D¨¦k¨¢ny, G¨¢bor T¨®th, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     (2¦Â,3¦Á,5¦Â,22R)-2,3,20,22,25-pentahydroxycholest- 7-en-6-one
C27H44O6     ÏàËÆ¶È:66.6%
Helvetica Chimica Acta          2008          Vol. 91          1640
Additional Minor Phytoecdysteroids of Serratula wolffii
Andr¨¢s Simon, Erika Liktor-Busa, G¨¢bor To¡ä th, Zolt¨¢n Kele, Judit Groska, and M¨¢ria B¨¢thori¨®
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     ponasterone A
    ÏàËÆ¶È:66.6%
Helvetica Chimica Acta          2008          Vol. 91          1640
Additional Minor Phytoecdysteroids of Serratula wolffii
Andr¨¢s Simon, Erika Liktor-Busa, G¨¢bor To¡ä th, Zolt¨¢n Kele, Judit Groska, and M¨¢ria B¨¢thori¨®
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     2¦Â,3¦Â,14¦Á,20¦Â,22¦Á,25¦Â-hexahydroxycholest-7-en-6-one
    ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          2007          43          672-677
SEPARATION AND IDENTIFICATION OF STEROIDAL COMPOUNDS WITH CYTOTOXIC ACTIVITY AGAINST HUMAN GASTRIC CANCER CELL LINES IN VITRO FROM THE RHIZOMES OF Paris polyphylla VAR. chinensis
Huang Yun, Cui Lijian, Zhan Wenhong Dou Yuhong,Wang Yongli, Wang Qiang, and Zhao Ding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     Sileneoside D
    ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          1998          34          602-604
PItYTOECDYSTEROIDS OF PLANTS OF THE Silene GENUS. XIX. THE STRUCTURE OF SILENEOSIDE G
Z. T. Sadykov and Z. Saatov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     2-deoxyecdysterone
    ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          1985          21          56-58
PHYTOECDYSTEROIDS OF PLANTS OF THE GENUS Silene.VIII. 2-DEOXYECDYSTERONE 3-ACETATE FROM Silene pvaemixta
Z. Saatov, M. B. Gorovits,N. D. Abdullaev, B. Z. Usmanov, and N. K. Abubakirov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     20,26-dihydroxyecdysone
    ÏàËÆ¶È:66.6%
Helvetica Chimica Acta          2009          92          753-761
Ecdysteroids from Silene viridiflora
Andr¨¢s Simon, No¨¦mi T¨®th, G¨¢bor T¨®th, Zolt¨¢n Kele, Judit Groska, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     ecdysterone
    ÏàËÆ¶È:66.6%
Acta Botanica Sinica          1996          38          399-405
Studieson the Chemical Constituents of the Leaves of Pseudotaxus chienii (Cheng)Cheng
Zhang Jun-zeng, Fang Qi-cheng and Liang Xiao-tian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     22-deoxyecdysterone
    ÏàËÆ¶È:66.6%
Acta Botanica Sinica          2001          43          316-318
Phytoecdysterones from Cucubalus baccifer
CHENG Yong-Xian, ZHOU Jun, TAN Ning-Hua, DING Zhong-Tao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     9¦Â,20-Dihydroxyecdysone
C27H45O8     ÏàËÆ¶È:66.6%
Steroids          2004          69          389-394
A new ecdysteroid with unique 9¦Â-OH and four other ecdysteroids from Silene italica ssp. nemoralis
Andr¨¢s Simon, Zita Pongr¨¢cz, G¨¢bor T¨®th, Marianna M¨¢k, Imre M¨¢th¨¦, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     22-Deoxy-integristerone A
    ÏàËÆ¶È:66.6%
Steroids          2004          69          389-394
A new ecdysteroid with unique 9¦Â-OH and four other ecdysteroids from Silene italica ssp. nemoralis
Andr¨¢s Simon, Zita Pongr¨¢cz, G¨¢bor T¨®th, Marianna M¨¢k, Imre M¨¢th¨¦, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     (20R,22R)-Cholest-5-ene-3¦Â,20,22-triol
C27H46O3     ÏàËÆ¶È:66.6%
Steroids          2004          69          483-493
Stereoselective synthesis of (22R)- and (22S)-castasterone/ponasterone A hybrid compounds and evaluation of their molting hormone activity
Bunta Watanabe, Yoshiaki Nakagawa, Takehiko Ogura, Hisashi Miyagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     Ajugasterone C
    ÏàËÆ¶È:66.6%
Steroids          2008          73          502-514
Additional minor ecdysteroid components of Leuzea carthamoides
Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
59 .     ponasterone A
    ÏàËÆ¶È:66.6%
China Journal of Chinese Materia Medica          2007          32          1421-1425
Non-taxoid chemical constituents from leaves of Taxus mairei
ZHANG Manli, HUO Changhong, DONG Mei, LIANG Chunhui, GU Yucheng, SHI Qingwen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
60 .     25-hydroxypanuosterone
C28H46O8     ÏàËÆ¶È:66.6%
Phytochemistry          1998          49          2109-2114
Ecdysteroid constituents of the mushroom Tapinella panuoides
Karel Vok¨¢, Milo Budnsky, Juraj Harmath¦Á, Jitka Kohoutov¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
61 .     ¦Â-ecdysone
C27H44O7     ÏàËÆ¶È:66.6%
Acta Pharmaceutica Sinica          1990          Vol 25          509-514
STEROIDAL SAPONINS FROM ASPARAGUS FILICINUS
Y Ding and CR Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
62 .     1-hydroxy-22-deoxy-20,21-didehydro-ecdysone
C27H42O6     ÏàËÆ¶È:66.6%
Magnetic Resonance in Chemistry          2010          48          386-391
Structure and stereochemistry of novel ecdysteroids from the roots of Serratula wolffii (pages 386¨C391)
M¨¢ria Tak¨¢cs, Andr¨¢s Simon, Erika Liktor-Busa, M¨¢ria B¨¢thori, Ferenc Zsila, Zsolt Bik¨¢di, P¨¦ter Horv¨¢th, G¨¢bor Veress, Andr¨¢s Gergely and G¨¢bor T¨®th
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
63 .     (20R,22R)-Cholest-5-ene-3¦Â,20,22-triol
    ÏàËÆ¶È:66.6%
Steroids          1999          64          385-395
An improved synthesis of(20R,22R)-cholest-5-ene-3¦Â,20,22-triol, an intermediate in steroid hormone formation and an activator of nuclear orphan receptor LXR¦Á
Benfang Ruan, William K. Wilson, George J. SchroepferJr.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
64 .     25-hydroxycholestero
    ÏàËÆ¶È:66.6%
Steroids          1994          59          310-317
Inhibitors of sterol synthesis. Effects of fluorine substitution at carbon atom 25 of cholesterol on its spectral and chromatographic properties and on 3-hydroxy-3-methylglutaryl coenzyme a reductase activity in CHO-K1 cells
William K. Wilson, Shankar Swaminathan, Frederick D. Pinkerton, Nicolas Gerst, George J. Schroepfer Jr.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
65 .     Ë®Áú¹ÇËØ B
C27H44O8     ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs          2006          37          1304-1306
°Î¶¾É¢»¯Ñ§³É·ÖµÄÑо¿
Àîά·å;ËÎÆôʾ;Ïîΰ;ÑîÊçÃô
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
66 .     ponasterone A
    ÏàËÆ¶È:66.6%
Chinese Journal of Medicinal Chemistry          2006          16          46-48
Isolation and identification of the chemical constituents from Mangrove plant Acrostichum a ureurm
MEI Wen-li, ZENG Yan-bo, DING Zhong-tao, DAI Hao-fu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
67 .     paristerone
    ÏàËÆ¶È:66.6%
Natural Product Research and Development          2003          15          93-97
ECDYSTEROIDS FROM THE STEMS OF DIPLOCLISIA GLAUCESCENS
HUANG Xiao chun GUO Yue wei ZHOU Wen liang ZUO Jian ping WANG Zheng tao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
68 .     20-hydroxyecdysone (6E)-oxime
C27H45NO7     ÏàËÆ¶È:66.6%
Russian Journal of Organic Chemistry          2006          42          1333-1339
Synthesis of 20-hydroxyecdysone oxime, its diacetonide, and their 14,15-anhydro derivatives
I. V. Galyautdinov, N. A. Ves¡¯kina, S. R. Afon¡¯kina, L. M. Khalilov and V. N. Odinokov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
69 .     Ë®Áú¹ÇçÞͪ B
C27H44O8     ÏàËÆ¶È:66.6%
Journal of Tropical and Subtropical Botany          2010          18          569-572
Chemical Constituents from Seeds of Achyranthes bidentata Blume.
DONG, Qinqin, YAN, Jian, ZHENG, Mengfei, HUAI, Huyin, TAN, Jianwen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
70 .     dyscusin A
C29H50O4     ÏàËÆ¶È:65.5%
Chemical & Pharmaceutical Bulletin          2011          59(10)          1303-1306
Dyscusins A-C, Three New Steroids from the Leaves of Dysoxylum cumingianum
Shin-ichiro KURIMOTO, Yoshiki KASHIWADA, Susan Lynne MORRIS-NATSCHKE, Kuo-Hsiung LEE, and Yoshihisa TAKAISHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
71 .     1¦Á,20¦Á-dihydroxyecdysone
    ÏàËÆ¶È:65.3%
Journal of Natural Products          2002          65          1194-1197
Ecdysteroids from a Zoanthus sp.
Apichart Suksamrarn,Aroon Jankam, Bongkoch Tarnchompoo, and Sumaitt Putchakarn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
72 .     2-deoxyecdysterone
C27H44O6     ÏàËÆ¶È:65.3%
Acta Botanica Yunnanica          2000          22(3)          351-357
Phytoecdysones from Porana discifera
ZHU Wei-Ming,YANG Xiao-Sheng,HE Hong-Ping,HAO Xiao-Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
73 .     20-hydroxyecdysone
C27H44O7     ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          1990          38          1927-1930
The Constituents of Cistanche tubulosa (SCHRENK) HOOK. f. II. : Isolation and Structures of a New Phenylethanoid Glycoside and a New Neolignan Glycoside
Fumio YOSHIZAWA,Takeshi DEYAMA,Nobuo TAKIZAWA,Khan USMANGHANI and Mansoor AHMAD
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
74 .     3¦Â-Hydroxy-23,24-bisnornorchol-5-en-22-carbaldehyde
    ÏàËÆ¶È:65.3%
Steroids          2005          70          551-562
Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids
Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Natalya B. Khripach, Alexey V. Antonchick, Andrey P. Antonchick, Bernd Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
75 .     (3¦Á,8¦Á,9¦Â,10¦Á,13¦Á,14¦Â,17¦Á,20S)-25-Hydroxycholesterol
C27H46O2     ÏàËÆ¶È:65.3%
Steroids          2006          71          484-488
Synthesis of ent-25-hydroxycholesterol
Emily J. Westover, Douglas F. Covey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
76 .     3¦Â ,25-dihydroxy-5-ene
C27H46O2     ÏàËÆ¶È:65.3%
Steroids          2009          74          81-87
A facile synthesis of C-24 and C-25 oxysterols by in situ generated ethyl(trifluoromethyl)dioxirane
Shoujiro Ogawa, Genta Kakiyama, Akina Muto, Atsuko Hosoda, Kuniko Mitamura, Shigeo Ikegawa, Alan F. Hofmann, Takashi Iida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
77 .     1¦Á,20R-dihydroxyecdysone
C38H44O8     ÏàËÆ¶È:65.3%
Phytochemistry          1998          49          2305-2310
1¦Á,20R-Dihydroxyecdysone from axyris amaranthoides
Satyajit D. Sarker, Vladimir Sik, Huw H. Rees, Laurence Dinan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
78 .     16-O-acetylgitoxigenin
    ÏàËÆ¶È:65.3%
Chinese Pharmaceutical Journal          2007          42          420-422
Studies on Chemical Constituents of Streptocaulon griffithii
ZHANG Lin, WANG Ye-fei, XU Li-zhen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
79 .     makisterone A
    ÏàËÆ¶È:64.2%
Chemistry & Biodiversity          2008          Vol. 5          707
Ecdysteroids from Vitex Species: Distribution and Compilation of Their 36C-NMR Spectral Data
Jos¨¦ G. Sena Filho, Jennifer Duringer, Gabriela L. A. Maia, Josean F. Tavares, Haroudo S. Xavier, Marcelo Sobral da Silva, Em.dio V. L. da-Cunha, and Jos¨¦ M. Barbosa-Filho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
80 .     makisterone A
    ÏàËÆ¶È:64.2%
Planta Medica          1985          51          40-42
Phytoecdysteroids of Diploclisia glaucescens Seed
R. W. Miller, J. C1ardy, J. Kozlowski, K. L. Mikolajczak, R. D. Plattner, R. G. Powell, C. R. Smith, D. Weisleder and Zheng Qi-Tai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
81 .     (3¦Â,23R)-ergost¦Á-5,24(28)-diene-3,23-diol
C28H46O2     ÏàËÆ¶È:64.2%
Chemistry & Biodiversity          2009          6          86-95
Revision of the Absolute Configuration at C(23) of Lanostanoids and Isolation of Secondary Metabolites from Formosan Soft Coral Nephthea erecta
Shi-Yie Cheng, Zhi-Hong Wen, Shang-Kewi Wang, Michael Y. Chiang, Ali A. H. El-Gamal, Chang-Feng Dai, and Chang-Yih Duh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
82 .     Makisterone A
C28H46O7     ÏàËÆ¶È:64.2%
Chemistry of Natural Compounds          1999          35          184-185
RI-IAPISTERONE D 20-ACETATE FROM THE SEEDS OF Leuzea carthamoides
E. B. Borovikova, G. S. Shangaraeva,and U. A. Baltaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
83 .     24-epi-Makisterone A
    ÏàËÆ¶È:64.2%
Steroids          2008          73          502-514
Additional minor ecdysteroid components of Leuzea carthamoides
Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
84 .     ergosta-5,24(24')-diene-3¦Â,4¦Â,20S-triol
C28H46O3     ÏàËÆ¶È:64.2%
Phytochemistry          1997          44          153-155
Ergosta-5, 24(24')-diene-3¦Â, 4¦Â, 20S-triol, an ergostane steroid from Dysoxylum malabaricum
T. R. Govindachari, G. N. Krishna Kumari, G. Suresh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
85 .     makisterone A
    ÏàËÆ¶È:64.2%
Korean Journal of Pharmacognosy          1998          29(4)          318-322
Studies on the Constituents from the Herbs of Ajuga multiflora (II)
Yu, Young-Jun; Do, Jae-Chul; Kwon, Soon-Youl; Son, Kun-Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
86 .     22E,24R-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â,9¦Á-tetraol
C28H46O4     ÏàËÆ¶È:64.2%
Chinese Journal of Medicinal Chemistry          2008          18          279-283
Chemical constituents from endophytic fungus S26 of Cephalotaxus hainanensis
CHEN Ping, WU Jiao, DAI Hao-fu, XIE Xiu-chao, MEI Wen-li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
87 .     (22E,24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Á,9¦Á-tetraol
C32H52O4     ÏàËÆ¶È:64.2%
Natural Product Research and Development          2007          19          436-438
Chemical Constituents of Basidiomycetes Russula subnigricans
GONG Qing-fang; ZHANG Yu-mei; TAN Ning-hua; CHEN Zuo-hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
88 .     20-hydroxyecdysone 2-mesylate
C28H46O9S     ÏàËÆ¶È:64.2%
Tetrahedron          2008          64          2626-2633
Functional group-mediated biotransformation by Curvularia lunata NRRL 2178: synthesis of 3-dehydro-2-deoxy-ecdysteroids from the 3-hydroxy-2-mesyloxy analogues
Chatchawan Changtam, Oratai Sukcharoen, Boon-ek Yingyongnarongkul, Nitirat Chimnoi, Apichart Suksamrarn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
89 .     Makisterone A
    ÏàËÆ¶È:64.2%
Journal of Agricultural and Food Chemistry          2001          49          2576-2578
Ecdysteroids of Quinoa Seeds (Chenopodium quinoa Willd.)
Nanqun Zhu, Hiroe Kikuzaki, Bret C. Vastano, Nobuji Nakatani, Mukund V. Karwe, Robert T. Rosen, and Chi-Tang Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
90 .     2, 3-acetonide ¦Â-ecdysterone
C30H48O7     ÏàËÆ¶È:63.3%
Acta Botanica Yunnanica          2000          22(3)          351-357
Phytoecdysones from Porana discifera
ZHU Wei-Ming,YANG Xiao-Sheng,HE Hong-Ping,HAO Xiao-Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
91 .     Integristeone A
    ÏàËÆ¶È:63.3%
Steroids          2008          73          502-514
Additional minor ecdysteroid components of Leuzea carthamoides
Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
92 .     limnantheoside B
C32H52O10     ÏàËÆ¶È:63.3%
Phytochemistry          1997          44          513-521
Ecdysteroid xylosides from Limnanthes douglasii
Satyajit D. Sarker, Jean-Pierre Girault, Ren¨¦ Lafont, Laurence N. Dinan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
93 .     20-hydroxyecdysone
    ÏàËÆ¶È:62.9%
Chemistry & Biodiversity          2008          Vol. 5          707
Ecdysteroids from Vitex Species: Distribution and Compilation of Their 13C-NMR Spectral Data
Jos¨¦ G. Sena Filho, Jennifer Duringer, Gabriela L. A. Maia, Josean F. Tavares, Haroudo S. Xavier, Marcelo Sobral da Silva, Em.dio V. L. da-Cunha, and Jos¨¦ M. Barbosa-Filho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
94 .     Shidasterone
    ÏàËÆ¶È:62.9%
Chemistry & Biodiversity          2008          Vol. 5          707
Ecdysteroids from Vitex Species: Distribution and Compilation of Their 17C-NMR Spectral Data
Jos¨¦ G. Sena Filho, Jennifer Duringer, Gabriela L. A. Maia, Josean F. Tavares, Haroudo S. Xavier, Marcelo Sobral da Silva, Em.dio V. L. da-Cunha, and Jos¨¦ M. Barbosa-Filho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
95 .     eurysterol A
C27H45O7SNa     ÏàËÆ¶È:62.9%
Journal of Natural Products          2007          70          846-848
Eurysterols A and B, Cytotoxic and Antifungal Steroidal Sulfates from a Marine Sponge of the Genus Euryspongia
Chollaratt Boonlarppradab* and D. John Faulkner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
96 .     eurysterol B
C27H43O7SNa     ÏàËÆ¶È:62.9%
Journal of Natural Products          2007          70          846-848
Eurysterols A and B, Cytotoxic and Antifungal Steroidal Sulfates from a Marine Sponge of the Genus Euryspongia
Chollaratt Boonlarppradab* and D. John Faulkner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
97 .     20-hydroxyecdysone
    ÏàËÆ¶È:62.9%
Journal of Natural Products          2002          65          1194-1197
Ecdysteroids from a Zoanthus sp.
Apichart Suksamrarn,Aroon Jankam, Bongkoch Tarnchompoo, and Sumaitt Putchakarn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
98 .     20-hydroxyecdysone
    ÏàËÆ¶È:62.9%
Journal of Natural Products          2002          65          1690-1692
Ecdysteroids of Vitex scabra Stem Bark
Apichart Suksamrarn, Saowanee Kumpun, and Boon-ek Yingyongnarongkul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
99 .     ¦Â-ecdysone
C27H44O7     ÏàËÆ¶È:62.9%
Acta Botanica Yunnanica          2000          22(4)          503-506
Phytoecdysones from Sida szechuensis
YAO Chun-Suo,XU Yun-Long
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
100 .     dcdysterone
    ÏàËÆ¶È:62.9%
Chemical & Pharmaceutical Bulletin          1994          42          1116-1122
Three New Furostanol Saponins from the Bulbs of Ipheion uniflorum
Osamu NAKAMURA,Yoshihiro MIMAKI,Yutaka SASHIDA,Tamotsu NIKAIDO and Taichi OHMOTO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-07-06 08:15:58
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

wangkaibo123

ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)

kerry

ÓÅÐã°æÖ÷

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¶¹¸ç: ¸ù¾Ýhttp://emuch.net/bbs/viewthread.php?tid=4896611£¬Î¢Æ×ÇóÖúÖ»½±ÀøµÚÒ»¸öÓ¦Öú¡£Ï´ÎÇëŬÁ¦¡£ 2013-07-06 14:06:12
haijiaotang: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-07-06 19:07:06
²éѯ½á¹û£º¹²²éµ½3718¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     2-deoxy-3-epi-4¦Â,20-dihydroxyecdysone
    ÏàËÆ¶È:92.3%
Russian Chemical Bulletin          2000          49          1923-1924
A new phytoecdysteroid
V. N. Odinokov, I. V. Galyautdinov, A. A. Fatykhov and L. M. Khalilov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     1¦Á,20R-hydroxyecdysone
    ÏàËÆ¶È:81.4%
Natural Product Research and Development          2002          14(1)          9-12
STUDY ON THE CHEMICAL CONSTITUENTS OF LYCHNIS CORONARIA
DAI Hao-fu; LIU Yu-qing; DENG Shi-ming; TAN Ning-hua; ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     20-hydroxyecdysone
    ÏàËÆ¶È:81.4%
Food Chemistry          2005          92          125-132
Nutritional and antinutritional composition of Kancolla seeds: an interesting and underexploited andine food plant
Irene Dini, Gian Carlo Tenore, Antonio Dini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     2-È¥Ñõ¼×¿ÇçÞͪ
    ÏàËÆ¶È:81.4%
Journal of Chinese Medicinal Materials          2010          33          1574-1576
Studies on the Chemical Constituents from the Roots of Tinospora sagittata var. yunnanensis(¢ò)
HUANG Xiang-zhong, CHENG Chun-mei, YIN Yan, GUO Jun-ming, LIANG Hui, DAI Yun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     20-hydroxyecdysone
    ÏàËÆ¶È:80.7%
Steroids          2002          67          127-135
Photochemical transformation of 20-hydroxyecdysone: production of monomeric and dimeric ecdysteroid analogues
Juraj Harmatha, Miloš Budĕš¨ªnsky, Karel Vok¨¢ĕ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     20-hydroxyecdysone
C27H44O7     ÏàËÆ¶È:80.7%
Phytochemistry          1998          49          2109-2114
Ecdysteroid constituents of the mushroom Tapinella panuoides
Karel Vok¨¢, Milo Budnsky, Juraj Harmath¦Á, Jitka Kohoutov¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     20-hydroxy-ecdysone
    ÏàËÆ¶È:80.7%
Phytochemistry          1994          37          707-711
Ecdysteroids from the roots of Leuzea carthamoides
Jaroslav P¨ªš, Miloš Bud¨§š¨ªnsky̌, Karel Vok¨¢č, V¨§ra Laudov¨¢, Juraj Harmatha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     20-hydroxyecdysone
    ÏàËÆ¶È:80.7%
Tetrahedron          1998          54          1657-1666
New ergostane type ecdysteroids from fungi. Ecdysteroid constituents of mushroom Paxillus atrotomentosus
Karel Vok¨¢č, Miloš Bud¨§š¨ªnsky, Juraj Harmatha, Jaroslav P¨ªš
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     2'-hydroxyecdysone
    ÏàËÆ¶È:77.7%
Phytochemistry          2003                   1179-1184
Ecdysteroids and other constituents from Sida spinosa L.
Faten M.M. Darwish, Manfred G. Reinecke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     integristerone A
    ÏàËÆ¶È:77.7%
Helvetica Chimica Acta          2009          92          753-761
Ecdysteroids from Silene viridiflora
Andr¨¢s Simon, No¨¦mi T¨®th, G¨¢bor T¨®th, Zolt¨¢n Kele, Judit Groska, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     integristerone A
    ÏàËÆ¶È:77.7%
Steroids          2004          69          389-394
A new ecdysteroid with unique 9¦Â-OH and four other ecdysteroids from Silene italica ssp. nemoralis
Andr¨¢s Simon, Zita Pongr¨¢cz, G¨¢bor T¨®th, Marianna M¨¢k, Imre M¨¢th¨¦, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     20-Hydroxyecdysone
    ÏàËÆ¶È:77.7%
Steroids          2008          73          502-514
Additional minor ecdysteroid components of Leuzea carthamoides
Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     20-hydroxyecdysone
    ÏàËÆ¶È:77.7%
China Journal of Chinese Materia Medica          2003          28          730-732
Studies on Chemical Constituents in Herb of Lamium maculatum L. var Kansuense
DENG Yanru, HE Li, LI Weiqi, WANG Hanqing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     20-hydroxyecdysone
    ÏàËÆ¶È:77.7%
Phytochemistry          1997          44          513-521
Ecdysteroid xylosides from Limnanthes douglasii
Satyajit D. Sarker, Jean-Pierre Girault, Ren¨¦ Lafont, Laurence N. Dinan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     ¦Â-ecdysone
C27H44O7     ÏàËÆ¶È:77.7%
Journal of Natural Medicines          2010          64          114-116
New naphthoquinone from the root of Lygodium japonicum (Thunb.) Sw.
Lijuan Chen, Guogang Zhang, Jie He, Jin Guan and Chunyuan Pan, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     ¦Â-ecdysone
C27H44O7     ÏàËÆ¶È:77.7%
Chinese Traditional and Herbal Drugs          2006          37          1304-1306
°Î¶¾É¢»¯Ñ§³É·ÖµÄÑо¿
Àîά·å;ËÎÆôʾ;Ïîΰ;ÑîÊçÃô
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     ¦Â-ecdysterone
C27H44O7     ÏàËÆ¶È:77.7%
Journal of China Pharmaceutical University          2006          37          487-490
Chemical constituents from Asparagus filicinus
WU Jia-jun; WANG Hao; YE Wen-cai; ZUO Xiao-feng; ZHAO Shou-xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
3Â¥2013-07-06 08:51:23
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ haijiaotang µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] Çóµ÷¼Á +4 ¿àÃüÈË¡£¡£¡£ 2026-04-18 4/200 2026-04-19 02:01 by ÑÌÓêÁ÷ÑÄ
[¿¼ÑÐ] 260Çóµ÷¼Á +4 Zyt1314520.. 2026-04-17 5/250 2026-04-18 08:28 by babysonlkd
[¿¼ÑÐ] ¼±Ðèµ÷¼Á +9 ¾ø²»·ÅÆú22 2026-04-15 10/500 2026-04-18 08:09 by chixmc
[¿¼ÑÐ] »¯¹¤Ñ§Ë¶294·Ö£¬Çóµ¼Ê¦ÊÕÁô +33 yzyzx 2026-04-12 37/1850 2026-04-17 23:00 by wunaiy88
[¿¼ÑÐ] 304Çóµ÷¼Á +7 castLight 2026-04-16 7/350 2026-04-17 20:05 by ¹ØÒ»ÕµµÆcd
[¿¼ÑÐ] 295·ÖÇóµ÷¼Á +5 ?ÒªÉϰ¶? 2026-04-17 5/250 2026-04-17 16:51 by fenglj492
[ÂÛÎÄͶ¸å] ÓÐûÓнÓÊձȽϿìµÄsciÆÚ¿¯Ñ½£¬×îºÃÔÚÒ»¸öÔÂÖ®Äڵģ¬ÑÐÈýº¢×ÓÇó±ÏÒµ 20+4 Ö®»¤×Å 2026-04-16 5/250 2026-04-17 10:02 by bobvan
[¿¼ÑÐ] 294Çóµ÷¼Á +14 µ­È»654321 2026-04-15 14/700 2026-04-16 21:01 by lpl364211
[¿¼ÑÐ] 291Çóµ÷¼Á +11 ¹ØÒä±±. 2026-04-14 11/550 2026-04-16 15:18 by jiahl2024
[¿¼ÑÐ] 26ҩѧר˶105500Çóµ÷¼Á +6 à¶¹þ¼ÓÓÍ 2026-04-13 7/350 2026-04-16 14:31 by zhouxiaoyu
[¿¼ÑÐ] Çóµ÷¼ÁÍÆ¼ö +8 СÄô°®Ñ§Ï° 2026-04-14 8/400 2026-04-16 07:22 by ѧԱJpLReM
[¿¼ÑÐ] 297£¬¹¤¿Æµ÷¼Á? +10 ºÓÄÏũҵ´óѧ-ÄÜ 2026-04-14 10/500 2026-04-15 21:50 by noqvsozv
[¿¼ÑÐ] ͨÐŹ¤³ÌÇóµ÷¼Á£¡£¡£¡ +6 zlb770521 2026-04-14 6/300 2026-04-15 20:00 by ѧԱJpLReM
[¿¼ÑÐ] 0854µ÷¼Á +13 ³¤¹­°Á 2026-04-12 16/800 2026-04-15 13:45 by fenglj492
[¿¼ÑÐ] 085600²ÄÁÏÓ뻯¹¤349·ÖÇóµ÷¼Á +16 Àîľ×Ó°¡¹þ¹þ 2026-04-12 17/850 2026-04-14 09:11 by fenglj492
[¿¼ÑÐ] 293Çóµ÷¼Á +16 ÎÒ°®¸ßÊý¸ßÊý°®Î 2026-04-12 18/900 2026-04-13 21:47 by ѧԱJpLReM
[¿¼ÑÐ] BÇø0809 £¬ÊýÒ»Ó¢Ò»£¬290 Çóµ÷¼Á +3 ãöΫ1111 2026-04-12 4/200 2026-04-13 20:35 by ѧԱJpLReM
[¿¼ÑÐ] 302Çóµ÷¼Á +10 Ò×£¡? 2026-04-13 10/500 2026-04-13 19:04 by lbsjt
[¿¼ÑÐ] Ò»Ö¾Ô¸Õã´óÉúÎï325·ÖÇóµ÷¼Á +9 zysheng 2026-04-12 9/450 2026-04-12 22:31 by yuyin1233
[¿¼ÑÐ] µ÷¼Á½áÊø +6 floriea 2026-04-12 8/400 2026-04-12 18:13 by zhouxiaoyu
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û